Skip to content

Intelligent Sensory Concept SA

SwitzerlandFDA applicant, unverified

Devices
1

What Intelligent Sensory Concept SA makes

Intelligent Sensory Concept SA manufactures the eLyx-PRO, a medical device designed for auditory assessment and rehabilitation, likely targeting hearing evaluation and customised sound amplification solutions.

The eLyx-PRO is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • eLyx-PRO Ref K162851

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Intelligent Sensory Concept SA have in the registry?

The registry currently lists 1 device for Intelligent Sensory Concept SA. Devices recorded under merged duplicate company entries are counted once.

Which registries list Intelligent Sensory Concept SA's devices?

Among its 1 most recently registered device, Intelligent Sensory Concept SA has devices listed in FDA 510(k) (1 device).

What risk classes do Intelligent Sensory Concept SA's devices fall under?

Among its 1 most recently registered device, the classes recorded for Intelligent Sensory Concept SA's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Intelligent Sensory Concept SA in the registry?

The most recently registered devices listed for Intelligent Sensory Concept SA include eLyx-PRO.

Generated automatically from registry data and not verified by a human reviewer.